Evidence map›Paper›PMID 20081856›Full record

SynthesisNature genetics2010

Meta-analysis of genome-wide association data identifies a risk locus for major mood disorders on 3p21.1.

Francis J McMahon, Nirmala Akula, Thomas G Schulze, Pierandrea Muglia, Federica Tozzi, Sevilla D Detera-Wadleigh, C J M Steele, René Breuer, Jana Strohmaier, Jens R Wendland and 11 more

Open access · greenAbstract readMeta-Analysis
In one paragraph

Synthesis in Nature genetics, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 92 papers, 13 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
92citing papers in PubMed, 13 pooled it
17.6field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

92 citing papers in PubMed, 13 syntheses or guidelines pooled it, 186 citations in OpenAlex.

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32 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

21 authors at 9 institutions in 8 countries.

Francis J McMahonUnit on the Genetic Basis of Mood & Anxiety Disorders, National Institute of Mental Health, National Institutes of Health, Department of Health and Human Services, Bethesda, Maryland, USA. mcmahonf@mail.nih.gov
Nirmala Akula
Thomas G Schulze
Pierandrea Muglia
Federica Tozzi
Sevilla D Detera-Wadleigh
C J M Steele
René Breuer
Jana Strohmaier
Jens R Wendland
Manuel Mattheisen
Thomas W Mühleisen
Wolfgang Maier
Markus M Nöthen
Sven Cichon
Anne Farmer
John B Vincent
Florian Holsboer
Martin Preisig
Marcella Rietschel
Bipolar Disorder Genome Study (BiGS) Consortium
University of Bonn · DENational Institutes of Health · USCentre for Addiction and Mental Health · CACentral Institute of Mental Health · DEGlaxoSmithKline (Netherlands) · NLKing's College London · GBMax Planck Institute of Psychiatry · DEUniversity of Lausanne · CHUniversity of Toronto · CA

Funding

Mapping genes that contribute to bipolar disorderZIAMH002810 · NIMH · NATIONAL INSTITUTE OF MENTAL HEALTH · PI MCMAHON, FRANCIS J · 2009 to 2025
$31.2M
Identification of Genes Involved in Major Mood DisordersZIAMH002843 · NIMH · NATIONAL INSTITUTE OF MENTAL HEALTH · PI MCMAHON, FRANCIS J · 2009 to 2025
$24.5M
Genomic Association Study of Bipolar DisorderR01MH078151 · NIMH · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI KELSOE, JOHN R. · 2007 to 2009
$5.5M
COLLABORATIVE GENOMIC STUDY OF BIPOLAR DISORDERR01MH059567 · NIMH · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI KELSOE, JOHN R. · 1998 to 2007
$1.8M
A Collaborative Genomic Study of Bipolar DisorderZ01MH002842 · NIMH · NATIONAL INSTITUTE OF MENTAL HEALTH · PI MCMAHON, FRANCIS J · 2004 to 2008
$1.2M
Genetic Linkage and Association in Bipolar DisorderZ01MH002843 · NIMH · NATIONAL INSTITUTE OF MENTAL HEALTH · PI MCMAHON, FRANCIS J · 2004 to 2008
$1.1M
A Collaborative Genomic Study of Bipolar DisorderZIAMH002842 · NIMH · NATIONAL INSTITUTE OF MENTAL HEALTH · PI MCMAHON, FRANCIS J · 2009 to 2010
$1.0M
Analysis of Whole Genome Association Data for Bipolar DisorderR01MH081804 · NIMH · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI KELSOE, JOHN R. · 2007 to 2007
$155k
Intramural NIH HHS Z01 MH002842Intramural NIH HHS Z01 MH002843Intramural NIH HHS ZIA MH002810NIMH NIH HHS MH059567NIMH NIH HHS MH078151NIMH NIH HHS MH081804NIMH NIH HHS R01 MH059567NIMH NIH HHS R01 MH078151NIMH NIH HHS R01 MH081804Wellcome Trust
6 · The paper itself

Abstract

The major mood disorders, which include bipolar disorder and major depressive disorder (MDD), are considered heritable traits, although previous genetic association studies have had limited success in robustly identifying risk loci. We performed a meta-analysis of five case-control cohorts for major mood disorder, including over 13,600 individuals genotyped on high-density SNP arrays. We identified SNPs at 3p21.1 associated with major mood disorders (rs2251219, P = 3.63 x 10(-8); odds ratio = 0.87; 95% confidence interval, 0.83-0.92), with supportive evidence for association observed in two out of three independent replication cohorts. These results provide an example of a shared genetic susceptibility locus for bipolar disorder and MDD.

Indexed as

Genetic Predisposition to DiseaseGenome-Wide Association StudyChromosomes, Human, Pair 3Genetic LociHumansMood DisordersPolymorphism, Single Nucleotide

Identifiers

PMID20081856
PMCPMC2854040
OpenAlexW2068388603

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.